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公开(公告)号:US20250003000A1
公开(公告)日:2025-01-02
申请号:US18680693
申请日:2024-05-31
Applicant: Natera, Inc.
Inventor: Solomon MOSHKEVICH , Bernhard ZIMMERMANN , Tudor Pompiliu CONSTANTIN , Huseyin Eser KIRKIZLAR , Allison RYAN , Styrmir SIGURJONSSON , Felipe ACOSTA ARCHILA , Ryan SWENERTON
IPC: C12Q1/6883
Abstract: The present disclosure provides methods for determining the status of an allograft within a transplant recipient from genotypic data measured from a mixed sample of DNA comprising DNA from both the transplant recipient and from the donor. The mixed sample of DNA may be preferentially enriched at a plurality of polymorphic loci in a way that minimizes the allelic bias, for example using massively multiplexed targeted PCR.
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12.
公开(公告)号:US20240229136A9
公开(公告)日:2024-07-11
申请号:US18279006
申请日:2022-02-24
Applicant: Natera, Inc.
Inventor: Zachary DEMKO , Ebad AHMED , Ryan SWENERTON , Paul VAN HUMMELEN
IPC: C12Q1/6883 , C12Q1/6869
CPC classification number: C12Q1/6883 , C12Q1/6869 , C12Q2600/156
Abstract: The present disclosure provides methods of amplifying and sequencing DNA, comprising: extracting cell-free DNA from a blood, plasma, serum or urine sample of a transplant recipient who has received transplantation of one or more organs including simultaneous or sequential transplantation of multiple organs, wherein the extracted cell-free DNA comprises donor-derived cell-free DNA and recipient-derived cell-free DNA; performing targeted amplification at 200-50,000 target loci in a single reaction volume using 200-50,000 primer pairs, wherein the target loci comprise polymorphic loci and non-polymorphic loci; sequencing the amplification products by high-throughput sequencing to obtain a sequencing reads and quantifying the amount of donor-derived cell-free DNA and the amount of total cell-free DNA based on the sequencing reads; and determining whether the amount of donor-derived cell-free DNA or a function thereof exceeds a cutoff threshold indicating transplant rejection or graft injury.
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公开(公告)号:US20230332221A1
公开(公告)日:2023-10-19
申请号:US18075180
申请日:2022-12-05
Applicant: Natera, Inc.
Inventor: Bernhard ZIMMERMANN , Ryan SWENERTON , Matthew RABINOWITZ , Styrmir SIGURJONSSON , George GEMELOS , Apratim GANGULY , Himanshu SETHI
IPC: C12Q1/6869 , C12Q1/6806
CPC classification number: C12Q1/6869 , C12Q1/6806 , C12Q2563/179 , C12Q2535/122 , C12Q2525/179
Abstract: The present disclosure provides methods and compositions for sequencing nucleic acid molecules and identifying individual sample nucleic acid molecules using Molecular Index Tags (MITs). Furthermore, reaction mixtures, kits, and adapter libraries are provided.
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公开(公告)号:US20220056509A1
公开(公告)日:2022-02-24
申请号:US17461298
申请日:2021-08-30
Applicant: Natera, Inc.
Inventor: Bernhard ZIMMERMANN , Raheleh SALARI , Ryan SWENERTON , Hsin-Ta WU , Himanshu SETHI
IPC: C12Q1/6827 , C12Q1/6886
Abstract: The invention provides methods for detecting single nucleotide variants in breast cancer, bladder cancer, or colorectal cancer. Additional methods and compositions, such as reaction mixtures and solid supports comprising clonal populations of nucleic acids, are provided. For example, provided here is a method for monitoring and detection of early relapse or metastasis of breast cancer, bladder cancer, or colorectal cancer, comprising generating a set of amplicons by performing a multiplex amplification reaction on nucleic acids isolated from a sample of blood or urine or a fraction thereof from a patient who has been treated for a breast cancer, bladder cancer, or colorectal cancer, wherein each amplicon of the set of amplicons spans at least one single nucleotide variant locus of a set of patient-specific single nucleotide variant loci associated with the breast cancer, bladder cancer, or colorectal cancer; and determining the sequence of at least a segment of each amplicon of the set of amplicons that comprises a patient-specific single nucleotide variant locus, wherein detection of one or more patient-specific single nucleotide variants is indicative of early relapse or metastasis of breast cancer, bladder cancer, or colorectal cancer.
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公开(公告)号:US20220251654A1
公开(公告)日:2022-08-11
申请号:US17616536
申请日:2020-05-29
Applicant: Natera, Inc.
Inventor: Dina M. HAFEZ , Prashanthi NATARAJAN , Raheleh SALARI , Ryan SWENERTON , Bernhard ZIMMERMANN
IPC: C12Q1/6881
Abstract: The disclosure herein provides methods and compositions for detecting or monitoring immune cell populations in biological samples. The methods and compositions disclosed herein are particularly useful for detecting or monitoring immune cell populations in patients suffering from a disease or undergoing treatment of a disease resulting in depletion of immune cells. In particular, the present disclosure provides method for using multiplex PCR combined with next-generation DNA sequencing to detect DNA containing recombined V(D)J gene segments which can be used to detect immune cells.
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公开(公告)号:US20220025455A1
公开(公告)日:2022-01-27
申请号:US17494726
申请日:2021-10-05
Applicant: Natera, Inc.
Inventor: Bernhard ZIMMERMANN , Ryan SWENERTON , Matthew RABINOWITZ , Styrmir SIGURJONSSON , George GEMELOS , Apratim GANGULY , Himanshu SETHI
IPC: C12Q1/6869 , C12Q1/6806
Abstract: The present disclosure provides methods and compositions for sequencing nucleic acid molecules and identifying individual sample nucleic acid molecules using Molecular Index Tags (MITs). Furthermore, reaction mixtures, kits, and adapter libraries are provided.
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公开(公告)号:US20210257048A1
公开(公告)日:2021-08-19
申请号:US16972930
申请日:2019-06-12
Applicant: Natera, Inc.
Inventor: Bernhard ZIMMERMANN , Raheleh SALARI , Ryan SWENERTON , Dina M. HAFEZ
IPC: G16B20/20 , C12Q1/6886
Abstract: A method for calling a mutation includes determining, for each target base of a plurality of target bases, a respective value for a background error parameter based on training data. The method further includes determining a motif-specific error model including the background error parameter by performing processes that include: identifying a respective motif for each target base of the plurality of target bases, grouping the plurality of target bases into a plurality of groups, each group corresponding to a particular motif, and determining, for each group, a respective motif-specific parameter value for the background error parameter based on the determined values for the background error parameter for the target bases included in each group. The method further includes calling a mutation using the motif-specific error model and sequencing information for a biological sample.
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公开(公告)号:US20210198733A1
公开(公告)日:2021-07-01
申请号:US17165592
申请日:2021-02-02
Applicant: Natera, Inc.
Inventor: Solomon MOSHKEVICH , Bernhard ZIMMERMANN , Tudor Pompiliu CONSTANTIN , Huseyin Eser KIRKIZLAR , Allison RYAN , Styrmir SIGURJONSSON , Felipe ACOSTA ARCHILA , Ryan SWENERTON
IPC: C12Q1/6869 , C12Q1/6851 , C12Q1/6876
Abstract: The present disclosure provides methods for determining the status of an allograft within a transplant recipient from genotypic data measured from a mixed sample of DNA comprising DNA from both the transplant recipient and from the donor. The mixed sample of DNA may be preferentially enriched at a plurality of polymorphic loci in a way that minimizes the allelic bias, for example using massively multiplexed targeted PCR.
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公开(公告)号:US20190309359A1
公开(公告)日:2019-10-10
申请号:US16418104
申请日:2019-05-21
Applicant: Natera, Inc.
Inventor: Bernhard ZIMMERMANN , Ryan SWENERTON , Matthew RABINOWITZ , Styrmir SIGURJONSSON , George GEMELOS , Apratim GANGULY , Himanshu SETHI
IPC: C12Q1/6869 , C12Q1/6806
Abstract: The present disclosure provides methods and compositions for sequencing nucleic acid molecules and identifying individual sample nucleic acid molecules using Molecular Index Tags (MITs). Furthermore, reaction mixtures, kits, and adapter libraries are provided.
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